drugset / Trial / NCT00123942

Trial of MEDI-507 in CD2-Positive Lymphoproliferative Disease

NCT00123942

Phase 1 Terminated 31 enrolled MedImmune LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine the maximum tolerated dose (MTD) and safety and tolerability of MEDI-507 in patients with CD2-positive lymphoproliferative disorders.

Timeline

Start
2004-04
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Siplizumab Monoclonal antibody